Cellulose powder was found to be a substrate favoring the deposition of cal
cite crystals from stable supersaturated solutions at pH 8.50 and at 25 deg
rees C, Kinetic analysis of the initial rates showed that they were proport
ional with the relative supersaturation with respect to calcite. Analysis o
f the dependence of the induction periods on the initial solution condition
s showed that the number of ions forming the critical nucleus was 5. The se
cond-order dependence of the rate of precipitation of calcite on cellulose
on the solution supersaturation suggested a surface controlled mechanism. T
he surface energy of the calcite nuclei growing on cellulose was calculated
to be 46 mJ m(-2) from the dependence of the induction time on the solutio
n supersaturation, The overgrowth of calcite on cellulose was done selectiv
ely on the macromolecules possibly through active sites formation at ioniza
ble functional groups (-OH), The nucleating capability of cellulose was fou
nd to be comparable with that of sulfonated polystyrene and significantly l
ower in comparison with sulfonated polystyrene divinyl benzene copolymer on
which vaterite was formed. This fact together with the selective growth of
the most stable calcite suggested that stereochemical factors are very imp
ortant in determining both the kinetics and the nature of the polymorph for
med. (C) 2000 Academic Press.